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Medpace Hiring Drug Safety Speialist in Pharmacovigilance

Published on

Medpace

1 Year

₹3L – ₹7L/yr

Navi Mumbai

B.Pharm, M.Pharm, Bsc, Msc, Pharm.D, Lifesciences, Nursing

Verified Job

Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

We are seeking a full-time, office-based Clinical Safety Coordinator to join our Clinical Safety department in India. This position involves handling and processing adverse events from all sources, including clinical trials and post-marketing surveillance. This role offers a fantastic opportunity to use your previous expertise and further develop your career.

Responsibilities:

  • Develop action plans for incoming safety-related calls.
  • Collect, process, and track adverse and serious adverse events.
  • Write detailed safety narratives.
  • Report various safety data.
  • Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.

Qualifications:

  • Bachelor’s degree in a healthcare-related field such as Nursing, Pharmacy, or Pharmacology.
  • Preferred: Clinical experience or experience in Clinical Research, case processing, and Post-Marketing Pharmacovigilance.
  • Proficient in English.
  • Strong knowledge of Microsoft® Office.
  • Broad knowledge of medical terminology.
  • Strong organizational and communication skills.

Application Link

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Medpace Hiring Drug Safety Speialist in Pharmacovigilance

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